Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("SPHINGOLIPIDOSIS")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 855

  • Page / 35
Export

Selection :

  • and

BASIC FINDINGS AND CURRENT DEVELOPMENTS IN SPHINGOLIPIDOSESPILZ H; HEIPERTZ R; SEIDEL D et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 47; NO 2; PP. 113-134; BIBL. 11 P.Article

ENZYMATIC ASPECTS OF THE LIPID STORAGE DISEASES.1978; ADV. EXPER. MED. BIOL.; U.S.A.; DA. 1978; VOL. 101; PP. 689-764; BIBL. DISSEM.; (MEET. ENZYMES LIPID METAB. PROC.; MONT STE-ODILE; 1977)Conference Paper

NIEMANN-PICK DISEASE: REPORT OF A CASE WITH SKIN INVOLVEMENTMARDINI MK; GERGEN P; MOHAMMED AKHTAR et al.1982; AMERICAN JOURNAL OF DISEASES OF CHILDREN; ISSN 0002-922X; USA; DA. 1982; VOL. 136; NO 7; PP. 650-651; BIBL. 6 REF.Article

SPHINGOLIPIDOSES: MOLECULAR MANIFESTATIONS AND BIOCHEMICAL STRATEGIESPENTCHEV PG; BARRANGER JA.1978; J. LIPID RES.; USA; DA. 1978; VOL. 19; NO 4; PP. 401-409; BIBL. 110 REF.Article

THE BIOCHEMICAL GENETICS OF THE HEXOSAMINIDASE SYSTEM IN MANBEUTLER E.1979; AMER. J. HUM. GENET.; USA; DA. 1979; VOL. 31; NO 2; PP. 95-105; BIBL. 74 REF.Article

MALADIES HEREDITAIRES DU METABOLISME DES MUCOPOLYSACCHARIDES, GLYCOPROTEINES ET SPHINGOLIPIDES. I: ANOMALIES BIOCHIMIQUESSALVAYRE R; THOUVENOT JP; DOUJTE BLAZY L et al.1979; REV. MED. TOULOUSE; FRA; DA. 1979; VOL. 15; NO 8; PP. 471-482; ABS. ENG; BIBL. 58 REF.Article

THE CLINICAL CLASSIFICATION OF CEROID-LIPOFASCINOSIS. A STATISTICAL APPROACH.REY PIAS JM; MORALES C; SERRATE A et al.1976; ARCH. SUISSES NEUROL. NEUROCHIR. PSYCHIATR.; SUISSE; DA. 1976; VOL. 119; NO 1; PP. 19-29; ABS. ALLEM. FR.; BIBL. 1 P. 1/2Article

EXPERIENCE OF ANTIOXIDANT TREATMENT IN NEURONAL CEROID-LIPOFUSCINOSIS OF SPIELMEYER-SJOEGREN TYPE.SANTAVUORI P; MOREN R.1977; NEUROPAEDIATRIE; DTSCH.; DA. 1977; VOL. 8; NO 4; PP. 333-344; ABS. ALLEM.; BIBL. 9 REF.Article

CELLULES DE KUPFFER ET DYSLIPOIDOSES.LAGERON A.1977; MED. CHIR. DIGEST.; FR.; DA. 1977; VOL. 6; NO 7; PP. 453-457; BIBL. 11 REF.Article

DE L'ANATOMIE PATHOLOGIQUE DES NEUROLIPIDOSESKOZAKOVA PB; KHOKHRINA NT; KALMIKOVA LG et al.1978; ZH. NEUROPATOL. PSIKHIATR. S.S. KORSAKOVA; SUN; DA. 1978; VOL. 78; NO 7; PP. 1095-1100; ABS. ENG; BIBL. 20 REF.Article

FAMILY REACTIONS, PHYSICIAN RESPONSES, AND MANAGEMENT ISSUES IN FATAL LIPID STORAGE DISEASES.SCHNEIDERMAN G; LOWDEN JA; RAE GRANT Q et al.1976; CLIN. PEDIATR.; U.S.A.; DA. 1976; VOL. 15; NO 10; PP. 887-890; BIBL. 5 REF.Article

MULTIPLE MOLECULAR FORMS OF ARYLSULFATASE A IN DIFFERENT FORMS OF METACHROMATIC LEUKODYSTROPHY (MLD)FARRELL DF; MACMARTIN MP; CLARK AF et al.1979; NEUROLOGY; USA; DA. 1979; VOL. 29; NO 1; PP. 16-20; BIBL. 18 REF.Article

PROGRESS IN INVESTIGATIONS OF SPHINGOLIPIDOSES.ADACHI M; SCHNECK L; VOLK BW et al.1978; ACTA NEUROPATHOL.; DEU; DA. 1978; VOL. 43; NO 1-2; PP. 1-18; BIBL. 5 P.Article

SPHINGOLIPIDOSESBRADY RO.1978; ANNU. REV. BIOCHEM.; USA; DA. 1978; VOL. 47; PP. 687-713; BIBL. 175 REF.Article

A POTENTIAL SOURCE OF ERROR IN THE ENZYMATIC DIAGNOSIS OF THE NEUROLIPIDOSES WHEN RADIOLABELLED SPHINGOLIPIDS ARE USED AS SUBSTRATES.POULOS A; POLLARD AC.1976; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1976; VOL. 73; NO 2; PP. 353-356; BIBL. 11 REF.Article

Isocortical pathology in type C Niemann-Pick disease. A combined Golgi-pigmentoarchitectonic studyBRAAK, H; BRAAK, E; GOEBEL, H. H et al.Journal of neuropathology and experimental neurology. 1983, Vol 42, Num 6, pp 671-687, issn 0022-3069Article

Maladie de Fabry = Fabry disease. An updatePORNEUF, M; SOTTO, A; PERRIN, P et al.La Semaine des hôpitaux de Paris. 1993, Vol 69, Num 21, pp 634-638, issn 0037-1777Article

A LYSOSOMAL STORAGE DISORDER IN MICE CHARACTERIZED BY A DUAL DEFICIENCY OF SPHINGOMYELINASE AND GLUCOCEREBROSIDASEPENTCHEV PG; GAL AE; BOOTH AD et al.1980; BIOCHIM. BIOPHYS. ACTA; ISSN 0006-3002; NLD; DA. 1980; VOL. 619; NO 3; PP. 669-679; BIBL. 26 REF.Article

THE ASSAY OF SPINGOLIPID HYDROLASES IN WHITE BLOOD CELLS WITH LABELLED NATURAL SUBSTRATESSVENNERHOLM L; HAKANSSON G; MANSSON JE et al.1979; CLIN. CHIM. ACTA; NLD; DA. 1979; VOL. 92; NO 1; PP. 53-64; BIBL. 19 REF.Article

ERKENNUNG UNHEILBARER, ERBLICHER STOFFWECHSEL-KRANKHEITEN VOR DER GEBURT: PRAENATALE DIAGNOSE VON FETTSTOFFWECHSELSTOERUNGEN = DIAGNOSTIC AVANT LA NAISSANCE DES MALADIES METABOLIQUES, HEREDITAIRES, INCURABLES: DIAGNOSTIC PRENATAL DES TROUBLES DU METABOLISME DES LIPIDESHARZER K.1979; MED. WELT; DEU; DA. 1979; VOL. 30; NO 48; PP. 1810-1816; BIBL. 10 REF.Article

DYSMYELINATION REVISITED.POSER CM.1978; ARCH. NEUROL.; USA; DA. 1978; VOL. 35; NO 7; PP. 401-408; BIBL. 2 P.Article

NEURONAL CEROID-LIPOFUSCINOSIS. STUDIES OF GRANULOCYTE ENZYME ACTIVITIES.MIN FU TSAN; GALE AN; MURPHY EA et al.1978; J. NEUROL. SCI.; NETHERL.; DA. 1978; VOL. 36; NO 1; PP. 13-24; BIBL. 24 REF.Article

A BENIGN DEFICIENCY OF TYPE B BETA -GALACTOSIDASE IN HUMAN LIVER.CHEETHAM PSJ; DANCE NE; ROBINSON D et al.1978; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1978; VOL. 83; NO 1-2; PP. 67-74; BIBL. 21 REF.Article

Animal and cellular models of sphingolipid storage disorders of humansGAL, A. E; WEIS, A. L; QUIRK, J. M et al.Chemistry and physics of lipids. 1986, Vol 42, Num 1-3, pp 199-207, issn 0009-3084Article

Enfermedades hereditarias lisosomales en México. III, Diagnóstico de laboratorio para esfingolipidosisELENA ZETINA, M; GONZALEZ-NORIEGA, A.Revista de investigacion clinica. 1991, Vol 43, Num 1, pp 52-60, issn 0034-8376Article

  • Page / 35